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Manufacturing Supervisor, Cell Culture Job
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| Employer Name: BiotechCrossing |
SpiderID: 2355242 |
| Location: Lexington, Massachusetts |
Date Posted: 7/9/2008 |
| Wage: |
Category: Biotech |
| Job Code: 6069513 |
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Job Description:
This includes overseeing a shift of Manufacturing Technicians and contractors during the start-up, commissioning, and validation of the Commercial Cell Culture and recovery areas.Following start-up, this position will be responsible for supervising a team of up to 8 Manufacturing Technicians in the day to day GMP operations of the Commercial Cell Culture areas. These include: Inoculum prep, bioreactor operations, recovery and daily process sampling.Responsibilities:Direct responsibilities include:* Assist the project teams to draft and review project documents such as, commissioning activities, validation plans, and training plans* Author and gain approval for standard operating procedures and process batch records relating to the Atlas manufacturing Cell Culture and recovery areas. * Lead and / or participate on teams responsible for drafting and approving global Atlas manufacturing SOP\'s.* Interface with Process Development (PD), Manufacturing Technical Services (MTS), and the Atlas Clinical and Commercial Manufacturing groups. * Actively participate on the Atlas Hiring and Assimilation team (interviewing, selecting, and on boarding staff)* Lead a team of Manufacturing Technicians in the Day to Day GMP operations of the Cell Culture and recovery areas. (May have additional reports during start-up, commissioning, and validation activities as required)* Performance Management: The Manufacturing Supervisor will be responsible for managing the performance of his / her direct reports through goal setting, mentoring, and scheduled reviews. * Manage the timely completion of processes and documentation to support plant floor operations. * Communicate effectively between all support functions, management, and staff.* Troubleshoot and diagnose process issues, elevate and communicate as needed. * Responsible for controlled document review.* SOP and batch record revisions * Regular collaboration with QA to ensure compliance. * Generate reports as required* Maintain training compliance.
For more information, please click here to visit us at BiotechCrossing
For further information, please visit us online at http://www.biotechcrossing.com
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Job Criteria:
Start Date:
Position Type: Full-Time Permanent
Years of Experience Required:
Education Required:
Overnight Travel:
Vacation Time:
Contact Information:
| Contact Name: - |
Company Type: Employer |
| Company: BiotechCrossing |
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| City: Pasadena |
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| State: California |
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| Zip: |
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Web Site: http://www.biotechcrossing.com
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